Clinical Research Study Coordinator - On-Site
PPG US ProPharma Group, LLC
PPG US ProPharma Group, LLC is seeking an On-Site Study Coordinator/Research Assistant in Raleigh, North Carolina. This role encompasses coordination of remote activities for clinical studies, where you will support communications, assist with screenings, and manage documentation compliant with regulations. The ideal candidate should possess a bachelor’s degree and relevant experience, ideally with 2 years in a study coordinator capacity. Strong organizational and communication skills are essential for success in this role. #J-18808-Ljbffr PPG US ProPharma Group, LLC
$35 - $42 per hour
...IQVIA LLC is seeking a Clinical Research Coordinator in Raleigh, NC. This full-time position requires the individual to manage clinical, operational, and data-related responsibilities for clinical trials. Qualifications include a Bachelor's degree and a minimum of 1+ year...WebsiteHourly payFull time- ...Clinical Research Coordinator I (On-site/ Raleigh) Position Description: The Clinical Research Coordinator (CRC) works under the guidance of the clinical... ..., playing a critical role in the conduct of the study. Essential Duties and Responsibilities Assist trial investigator...WebsiteFlexible hours
- ...Clinical Research Coordinator II – Wake Research Location: Raleigh, NC. Position is on-site. Job Description The Clinical Research Coordinator II (CRC II) is an experienced research... ...mentors research staff and contributes to study oversight, workflow optimization, and team...WebsiteFlexible hours
- ...Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient... ...trial(s) from start up through study close out in accordance with the... ...and Velocity’s SOPs Implement and coordinate assigned clinical trials including...WebsiteWork at officeFlexible hours
- ...Clinical Research Coordinator II (On-site) Full-time M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting... ...in accordance with regulatory compliance. Conducting studies since 1984, M3 Wake Research owns a proprietary patient...WebsiteFull timeFlexible hours
- ...Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient... ...trials in accordance with the study protocol,GCP, and Velocity's... ...Guidelines and Velocity's SOPs Coordinate, with supervision, assigned clinical...WebsiteWork at officeFlexible hours
$27 - $32 per hour
...Clinical Research Coordinator Position Summary: The Clinical Research Coordinator will be primarily responsible... ...and related regulations. A lead study coordinator will have oversight of... ...direction of the Primary Investigator and Site Lead. Since this is primarily a...WebsiteContract workTemporary work$35 - $42 per hour
Clinical Research Coordinator - Raleigh, NC Work Setup: On‑site Employment Type: Full‑time Position Overview We are seeking a Clinical Research Coordinator (CRC)... ...and biological sample collection in accordance with study protocols Coordinate daily clinical trial...WebsiteHourly payFull timePart time$31.25 per hour
Position Overview The Clinical Research Coordinator will support the department’s first research network in the world dedicated to improving... ...will play an important role in supporting multi-site clinical research studies. The Coordinator will assist with study operations,...WebsiteFull timeTemporary workPart timeWork at officeImmediate start$35 - $42 per hour
IQVIA in Raleigh, NC is seeking a Clinical Research Coordinator to support clinical trials under a Principal Investigator. The role involves managing clinical, operational, and data-related responsibilities while adhering to regulatory requirements. Ideal candidates should...WebsiteHourly payVisa sponsorship- ...healthcare industry… Revival Research Institute, LLC was... ...of data for our clinical research trials. As Revival... ...Clinical Research Coordinator with a minimum of2yearofclinicalexperience... ...our Woman's Health site. Someone with a... ...and manage multiple studies.They are...WebsiteWork at office
- ...for implementation of one or more clinical trials and all activities from study start-up through database lock, ensuring... ..., and operational aspects of site investigator grants and grant... ...content to the study protocol and coordinates completion of QC review of the protocol...WebsiteContract workRemote work
$95.5k - $159k
...sponsor liaison and advocate, the Clinical Project Manager will plan,... ...or therapeutic area clinical research projects. Utilizing existing templates... ...project tasks that include site monitoring, CRF and database... ...Degree in a relevant field of study (Health Sciences, Clinical...WebsiteLocal areaWork from home- Overview Clinical Project Manager II - Virology (Sponsor Dedicated... ...operational details that keep studies running successfully day to day... ..., and cross-functional coordination Maintain direct involvement... ...operational deliverables, and site-related activities Oversee site...WebsiteRemote jobContract workWork from home2 days per week3 days per week
- Worldwide Clinical Trials Holdings, Inc. is seeking an experienced leader for the Clinical Site Management team. The role involves providing direction from study start to closure and acting as the primary contact... ...experience as a Clinical Research Associate, strong...WebsiteWorldwide
- ...Description M3 Wake Research, an M3USA Company, is an integrated... ...premier investigational sites meeting the clinical research needs of global... ...compliance. Conducting studies since 1984, M3 Wake... ...for a Clinical Research Coordinator at Wake Research, an M3...WebsiteFlexible hours
- ...Job Description POSITION TITLE: Clinical Research Coordinator I DEPARTMENT: Global Project Delivery... ...with a team of other CRCs to clinical sites as assigned to conduct world-class research... ...information during clinical research study visits while ensuring compliance with...WebsiteDaily paidFull timeContract workFlexible hours
$27 - $32 per hour
...Carolina, US* Position Summary: The Clinical Research Coordinator will be primarily responsible for conducting... ...and related regulations. A lead study coordinator will have oversite of assigned... ...of the Primary Investigator and Site Lead. Since this is primarily a patient...WebsiteContract workTemporary workWork at officeRelocation$114k - $210.9k
...Experienced Clinical Trial Manager - Full-Service Job... ...Responsibilities Responsible for site management oversight,... ...(RACT). Reviews the study scope of work, budget... ...and Data Management to coordinate delivery handoffs and... ...conduct of a clinical research project. Demonstrates critical...WebsiteContract workFlexible hours- Syneos Health/ inVentiv Health Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site interactions and ensure safety and compliance within clinical trials. Responsibilities include managing project timelines, supporting team training, and maintaining...Website
- ...North Carolina State University is seeking a Clinical Research Coordinator to support groundbreaking research dedicated to improving treatments for... ...survivors of sexual assault. This role involves managing study operations, participant recruitment, and ensuring compliance...
- Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator II to manage clinical trials from start to finish, ensuring adherence to protocols and regulatory guidelines. Responsibilities include preparing and submitting regulatory documents, managing subject...
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- Job Summary The On‑Site Study Coordinator/Research Assistant position is responsible for the coordination and support of remote site activities for... ..., evaluate and respond to system queries and monitor clinical databases as assigned. Establish and maintain timely Site...WebsiteRemote work
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- Aerogen is looking for a Clinical Trial Manager (CTM) in Morrisville, NC to manage multiple aspects of clinical trials, including study start-up, site management, and vendor oversight. The CTM will ensure compliance with regulatory standards, handle subject safety, and...Website
- Senior Clinical Trial Manager - Remote, US ICON plc is a world-leading... ...intelligence and clinical research organization. We’re proud to... ...all clinical aspects of the studies. Your expertise and... ...others. Visit our careers site to read more about the benefits...WebsitePermanent employmentRemote workFlexible hours
- ...solutions organization in Morrisville, NC, is seeking an Experienced Clinical Trial Manager to oversee clinical trials, ensuring compliance... ...leadership, problem-solving skills, and the ability to manage site interactions effectively. You will lead strategic planning and collaboration...Website
$49 - $59 per hour
...Syneos Health, Inc. is seeking a Clinical Research Project Coordinator in Morrisville, NC to oversee various phases of clinical trials. Candidates must have a Registered Nurse or Bachelor's Degree and at least 1 year of clinical research experience. Responsibilities include...Hourly pay
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